Process for preparing polyamine derivative and intermediates thereof

ABSTRACT

The present invention provides a novel process for preparing polyamine derivatives and pharmaceutically acceptable salts thereof, which are useful as antineoplastic agents and to novel intermediates thereof.

This is a continuation of application Ser. No. 08/508,097, filed Jul.27, 1995, which is a continuation of Ser. No. 08/358,053, filed Dec. 16,1994, now abandoned, which is a continuation of Ser. No. 08/133,484,filed Oct. 7, 1993, now abandoned, which is herein incorporated byreference.

The present invention relates to a novel process for preparing polyaminederivatives and pharmaceutically acceptable salts thereof, which areuseful as antineoplastic agents European Patent Application 0 311 068,Publication Date Mar. 4, 1989! and to novel intermediates thereof.

The process and intermediates of the present invention provide a novelmethod for preparing antineoplastic polyamine derivatives.

SUMMARY OF THE INVENTION

The present invention provides a novel process for preparing a compoundof the formula ##STR1## wherein m is 6, 7, 8, or 9,

R₁, R₂, R₃, R₄, R₅, and R₆, are each independently hydrogen or a C₁ -C₃alkyl group with the proviso that the total number of carbon atomsincorporated by all the groups R₁, R₂, R₃, R₄, R₅, or R₆ may not exceed6,

Z is hydrogen, methyl, or ethyl;

and pharmaceutically acceptable salts thereof comprising the steps of:

(a) reacting a compound of the formula ##STR2## wherein m is 6, 7, 8, or9,

R₁, R₂, R₃, R₄, R₅, and R₆, are each independently hydrogen or a C₁ -C₃alkyl group with the proviso that the total number of carbon atomsincorporated by all the groups R₁, R₂, R₃, R₄, R₅, or R₆ may not exceed6;

with an appropriate aldehyde to give a bis-hexahydropyrimidinederivative;

(b) reacting the bis-hexahydropyrimidine derivative with an appropriateacylating agent to give a bis-acylhexahydropyrimidine derivative;

(c) reacting the bis-acylhexahydropyrimidine derivative with anappropriate reducing agent to give a bis-alkylhexahydropyrimidinederivative;

(d) reacting the bis-alkylhexahydropyrimidine derivative with anappropriate solvolysis agent.

In addition, the present invention provides for novelbis-acylhexahydropyrimidine derivatives of the formula: ##STR3## whereinm is 6, 7, 8, or 9,

R₁, R₂, R₃, R₄, R₅, and R₆, are each independently hydrogen or a C₁ -C₃alkyl group with the proviso that the total number of carbon atomsincorporated by all the groups R₁, R₂, R₃, R₄, R₅, or R₆ may not exceed6,

Z is hydrogen, methyl, or ethyl,

Y is hydrogen, C₁ -C₆ alkyl, phenyl, or substituted phenyl

In addition, the present invention provides for novelbis-alkylhexahydropyrimidine derivatives of the formula: ##STR4##wherein m is 6, 7, 8, or 9,

R₁, R₂, R₃, R₄, R₅, and R₆, are each independently hydrogen or a C₁ -C₃alkyl group with the proviso that the total number of carbon atomsincorporated by all the groups R₁, R₂, R₃, R₄, R₅, or R6 may not exceed6,

Z is hydrogen, methyl, or ethyl,

Y is hydrogen, C₁ -C₆ alkyl, phenyl, or substituted phenyl.

DETAILED DESCRIPTION OF THE INVENTION

As used in this application:

a) the designation "" refers to a bond for which the stereochemistry isnot designated.

b) the term "pharmaceutically acceptable salts" refers to acid additionsalts;

c) the term "C₁ -C₃ alkyl" refers to a branched or straight chainedalkyl radical containing from 1-3 carbon atoms, such as methyl, ethyl,n-propyl, and isopropyl;

d) the term "C₁ -C6 alkyl" refers to a branched or straight chained, orcyclic alkyl radical containing from 1-6 carbon atoms, such as methyl,ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, n-pentyl,cyclopentyl, n-hexyl, cyclohexyl, and the like;

e) the term "phenyl" refers to; ##STR5## f) the term "substitutedphenyl" refers to; ##STR6## wherein Q, W, and X are independently chosenfrom the group consisting of; hydrogen, C₁ -C₄ alkyl, C₁ -C₄ alkoxy, orhalogen.

The expression "pharmaceutically acceptable acid addition salts" isintended to apply to any non-toxic organic or inorganic acid additionsalt of the polyamine derivatives or any of its intermediates.Illustrative inorganic acids which form suitable salts includehydrochloric, hydrobromic, sulphuric, and phosphoric acid and acid metalsalts such as sodium monohydrogen orthophosphate, and potassium hydrogensulfate. Illustrative organic acids which form suitable salts includethe mono-, di-, and tricarboxylic acids. Illustrative of such acids arefor example, acetic, glycolic, lactic, pyruvic, malonic, succinic,glutaric, fumaric, malic, tartaric, citric, ascorbic, maleic,hydroxymaleic, benzoic, hydroxy-benzoic, phenylacetic, cinnamic,salicyclic, 2-phenoxy-benzoic, and sulfonic acids such asp-toluenesulfonic acid, methane sulfonic acid and 2-hydroxyethanesulfonic acid. Such salts can exist in either a hydrated orsubstantially anhydrous form.

In compounds of the Formulas I, II, III, and IV there are two each ofthe groups R₁, R₂, R₃, R₄, R₅, and R₆. In compounds of the Formulas I,II, III, and IV in which one or more of the groups R₁, R₂, R₃, R₄, R₅,and R6 is other than hydrogen; the total number of carbons incorporatedby all the groups R₁, R₂, R₃, R₄, R5, or R₆ may not exceed 6.Illustrative examples of compounds of Formula I which can be prepared bythe present process containing groups R₁, R₂, R₃, R₄, R₅, and R₆ isother than hydrogen are;

ZCH₂ NHCH(CH₃)CH₂ CH₂ NH(CH₂)_(m) NHCH₂ CH₂ (CH₃)CHNHCH₂ Z,

ZCH₂ NHCH(CH₂ CH₃)CH₂ CH₂ NH(CH₂)_(m) NHCH2CH2(CH₂ CH₃)CHNHCH₂ Z,

ZCH₂ NHCH(CH₂ CH₂ CH₃)CH₂ CH₂ NH(CH₂)_(m) NHCH2CH₂ (CH₂ CH₂ CH₃)CHNHCH₂Z,

ZCH₂ NHCH₂ CH₂ CH(CH₃)NH(CH2)_(m) NH(CH₃)CHCH₂ CH₂ NHCH₂ Z,

ZCH₂ NHC(CH₃)₂ CH₂ CH₂ NH(CH₂)_(m) NHCH₂ CH₂ (CH₃)₂ CNHCH₂ Z,

ZCH₂ NHCH₂ CH(CH₃)CH₂ NH(CH₂)_(m) NHCH₂ (CH₃)CHCH₂ NHCH₂ Z.

These illustrative examples are not intended to limit the presentinvention in any way.

As is appreciated by one of ordinary skill in the art the compounds ofthe Formulas I, II, III, and IV in which one or more of the groups R₁,R₂, R₃, R₄, R₅, and R₆ are not hydrogen may exist as stereoisomersdepending on the nature of R₁, R₂, R₃, R₄, R₅, and R6. In addition, thecompounds of the Formulas II, III, and IV may exist as stereoisomersdepending on the nature of R₁, R₂, R₃, R₄, R₅, R₆, and Y. Any referencein this application to one of the compounds of the Formulas I, II, III,and IV is meant to encompass either specific stereoisomers or a mixtureof stereoisomers. The Cahn-Ingold-Prelog designation of (R)- and (S)-for the stereochemistry of compounds represented by Formula I, II, III,and IV depends on the nature of R₁, R₂, R₃, R₄, R₅, R₆, and Y. Thespecific stereoisomers can be prepared by stereospecific synthesis orcan be separated and recovered by techniques known in the art, such aschromatography on chiral stationary phases, amide formation with achiral acid followed by separation of the resultant diastereomericamides and hydrolysis to the desired stereoisomer, or fractionalrecrystallization of addition salts formed by reagents used for thatpurpose, as described in "Enantiomers, Racemates, and Resolutions", J.Jacques, A. Collet, and S. H. Wilen, Wiley (1981).

Examples of compounds encompassed by the present invention include:

1,7-Bis-(3-acetylhexahydropyrimidin-1-yl)-heptane;

1,7-Bis-(3-formylhexahydropyrimidin-1-yl)-heptane;

1,7-Bis-(3-propionylhexahydropyrimidin-1-yl)-heptane;

1,6-Bis-(3-acetylhexahydropyrimidin-1-yl)-hexane;

1,6-Bis-(3-formylhexahydropyrimidin-1-yl)-hexane;

1,6-Bis-(3-propionylhexahydropyrimidin-1-yl)-hexane;

1,8-Bis-(3-acetylhexahydropyrimidin-1-yl)-octane;

1,8-Bis-(3-formylhexahydropyrimidin-1-yl)-octane;

1,8-Bis-(3-propionylhexahydropyrimidin-1-yl)-octane;

1,9-Bis-(3-acetylhexahydropyrimidin-1-yl)-nonane;

1,9-Bis-(3-formylhexahydropyrimidin-1-yl)-nonane;

1,9-Bis-(3-propionylhexahydropyrimidin-1-yl)-nonane;

(R, R)-1,7-Bis-(3-acetyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

(R, R)-1,7-Bis-(3-formyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

(R, S)-1,7-Bis-(3-formyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

(R, R)-1,7-Bis-( 3-propionyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

(S, S)-1,7-Bis-(3-acetyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

(S, S)-1,7-Bis-(3-formyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

(S, S)-1,7-Bis-(3-propionyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

1,7-Bis-(3-ethylhexahydropyrimidin-1-yl)-heptane;

1,7-Bis-(3-methylhexahydropyrimidin-1-yl)-heptane;

1,7-Bis-(3-propylhexahydropyrimidin-1-yl)-heptane;

1,6-Bis-(3-ethylhexahydropyrimidin-1-yl)-hexane;

1,6-Bis-(3-methylhexahydropyrimidin-1-yl)-hexane;

1,6-Bis-(3-propylhexahydropyrimidin-1-yl)-hexane;

1,8-Bis-(3-ethylhexahydropyrimidin-1-yl)-octane;

1,8-Bis-(3-methylhexahydropyrimidin-1-yl)-octane;

1,8-Bis-(3-propylhexahydropyrimidin-1-yl)-octane;

1,9-Bis-(3-ethylhexahydropyrimidin-1-yl)-nonane;

1,9-Bis-(3-methylhexahydropyrimidin-1-yl)-nonane;

1,9-Bis-(3-propylhexahydropyrimidin-1-yl)-nonane;

(R, R)-1,7-Bis-(3-ethyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

(R, R)-1,7-Bis-(3-methyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

(R, S)-1,7-Bis-(3-methyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

(R, R)-1,7-Bis-(3-propyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

(S, S)-1,7-Bis-(3-ethyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

(S, S)-1,7-Bis-(3-methyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

(S, S)-1,7-Bis-(3-propyl-4-methyl-hexahydropyrimidin-1-yl)-heptane;

1,7-Bis- (3-ethylamino)propyl!-heptanediamine;

1,7-Bis- (3-methylamino)propyl!-heptanediamine;

1,7-Bis- (3-propylamino)propyl!-heptanediamine;

1,6-Bis- (3-ethylamino)propyl!-hexanediamine;

1,6-Bis- (3-methylamino)propyl!-hexanediamine;

1,6-Bis- (3-propylamino)propyl!-hexanediamine;

1,8-Bis- (3-ethylamino)propyl!-octanediamine;

1,8-Bis- (3-methylamino)propyl!-octanediamine;

1,8-Bis- (3-propylamino)propyl!-octanediamine;

1,9-Bis- (3-ethylamino)propyl!-nonanediamine;

1,9-Bis- (3-methylamino)propyl!-nonanediamine;

1,9-Bis- (3-propylamino)propyl!-nonanediamine;

(R, R)-1,7-Bis- (3-ethylamino)-3-methyl-propyl!-heptanediamine;

(R, R)-1,7-Bis- (3-methylamino)-3-methyl-propyl!-heptanediamine;

(R, S)-1,7-Bis- (3-methylamino)-3-methyl-propyl!-heptanediamine;

(R, R)-1,7-Bis- (3-propylamino)-3-methyl-propyl!-heptanediamine;

(S, S)-1,7-Bis- (3-ethylamino)-3-methyl-propyl!-heptanediamine;

(S, S)-1,7-Bis- (3-methylamino)-3-methyl-propyl!-heptanediamine;

(S, S)-1,7-Bis- (3-propylamino)-3-methyl-propyl!-heptanediamine.

A general synthetic procedure for preparing polyamine derivatives,bis-acylhexahydropyrimidine derivatives, andbis-alkylhexahydropyrimidine derivatives is set forth in Scheme A. InScheme A, all substituents unless otherwise indicated, are as previouslydefined. Starting materials, reagents, techniques, and procedures usedin Scheme A are well known and appreciated by one of ordinary skill inthe art. ##STR7##

The compounds of structure (1) in which m and R₁, R₂, R₃, R₄, R₅, and R₆are as defined above can be obtained by methods known in the art.Specifically, compounds of structure (1) in which m is 6,7,8, and 9; andR₁, R₂, R₃, R₄, R₅, and R₆ are hydrogen can be obtained by the methodsin Prakash et al, U.S. Pat. No. 5,109,024, M. L Edwards et al, J. Med.Chem. 34, 2414-2420 (1991), and M. L Edwards et al, J. Med. Chem. 33,1369-1375 (1990). The compounds of structure (1) in which m is 6,7,8,and 9; and R₁, R₂, R₃, R₄, R₅, and R₆ are independently C₁ -C₃ alkyl canbe obtained by methods known in the art or by methods known analogouslyin the art in Prakash et al, U.S. Pat. No. 5,109,024, M. L Edwards etal, J. Med. Chem. 34, 2414-2420 (1991), M. L Edwards et al, J. Med.Chem. 33, 1369-1375 (1990), M. L Edwards et al, Tet, Lets. 31, 3417-3420(1990), F. J. Weiberth and S. S. Hall, J. Org. Chem.51, 5338-5341(1986), and S. Nagarajan and B. Ganem, J. Org. Chem.51, 4856-4861(1986).

In step a, a compound of structure (1) is is contacted with anappropriate aldehyde to form a bis-hexahydropyrimidine of structure (2).

For example, a compound of structure (1) or a salt of a polyamine ofstructure (1) is contacted with an appropriate aldehyde. Appropriatealdehydes are well known in the art and include but are not limited tobenzaldehyde and formaldehyde and formaldehyde equivalents, such asparaformaldehyde, dimethoxymethane and polyoxymethylene withformaldehyde being preferred. The reaction is carried out in a solvent,such as water, dioxane, methanol, or ethanol with water being preferred.In reactions were a salt of a compound of structure (1) is the startingmaterial; an equimolar amount of a suitable base is used to neutralizethe acid that forms a polyamine salt. Suitable bases include but are notlimited to sodium hydroxide, potassium hydroxide, and triethylamine. Thereaction is carried out at temperatures of from 0° C. to 60° C. Thereaction require from 1 to 24 hours. Bis-hexahydropyrimidine derivativesof structure (2) may be isolated from the reaction zone by extractionand evaporation, as is well known in the art. Bis-hexahydropyrimidinederivatives of structure (2) may be used after isolation without furtherpurification or may be purified by techniques well known in the art,such as chromatography and recrystallization.

In step b, a bis-hexahydropyrimidine derivative of structure (2) iscontacted with an appropriate acylating agent to form abis-acylhexahydropyrimidine of structure (3).

For example, a bis-hexahydropyrimidine derivative of structure (2) iscontacted with an appropriate acylating agent. An appropriate acylatingagent is one that transfers an acyl group. Appropriate acylating agentsare well known in the art and include but are not limited to formicacid, acetic acid, propionic acid, formic-acetic mixed anhydride, aceticanhydride, propionic anhydride, acetyl chloride, propionyl chloride, andacetyl-O-hydroxysuccinimide. When the appropriate acylating agent is anacid the reaction is carried out in the presence of a reagent thatassists in the coupling of acids and amines, such as1,3-dicyclohexylcarbodiimide or2-ethyl-l-ethoxycarbonyl-1,2-dihydroquinoline. When the appropriateacylating agent is an acid chloride or an acid anhydride the reaction iscarried out in the presence of a base, such as triethylamine,diisopropylethylamine, or pyridine to neutralize the acid which isliberated during the course of the reaction. The reaction is carried outin a solvent, such as tetrahydrofuran, dichloromethane, ethyl acetate,acetonitrile, or dioxane. The reaction is carried out at temperatures ofbetween 10° C. and the refluxing temperature of the solvent.Bis-acylhexahydropyrimidine derivatives of structure (3) may be isolatedfrom the reaction zone by extraction and evaporation, as is well knownin the art. Bis-acylhexahydropyrimidine derivatives of structure (3) maybe used after isolation without further purification or may be purifiedby techniques well known in the art, such as chromatography andrecrystallization.

In step c, a bis-acylhexahydropyrimidine derivatives of structure (3) iscontacted with an appropriate reducing agent to form abis-alkylhexahydropyrimidine derivatives of structure (4).

For example, a bis-acylhexahydropyrimidine derivatives of structure (3)is contacted with a molar excess of an appropriate reducing agent, suchas lithium aluminum hydride, borane, or a borane complex, such as boranedimethylsulfide. The reaction is carried out in a suitable solvent.Suitable solvents for hydride reductions are well known in the art, suchas toluene, diethyl ether, methyl t-butyl ether, and tetrahydrofuran(THF). The reaction is carried out at a temperatures of 10° C. to therefluxing temperature of the solvent. The bis-alkylhexahydropyrimidinederivatives of structure (4) can be isolated from the reaction zone asis well known in the art by quenching, filtration, extraction, andevaporation to give bis-alkylhexahydropyrimidine derivatives ofstructure (4). Bis-alkylhexahydropyrimidine derivatives of structure (4)can be used after isolation without further purification or may bepurified by techniques well known in the art, such as chromatography andrecrystallization.

In step d, a bis-alkylhexahydropyrimidine derivatives of structure (4)is contacted with an appropriate solvolysis agent to give a compound ofstructure (5) as a salt thereof.

An appropriate solvolysis agent is a protonic acid usually in thepresence of a protic solvent, such as water, methanol, ethanol,water/methanol mixtures, or water/ethanol mixtures.

For example, a bis-alkylhexahydropyrimidine derivatives of structure (4)is contacted with an acid, such as hydrochloric acid, hydrobromic acid,or trifluoroacetic acid to give a compound of structure (5) as a salt.The reaction may be carried out in a solvent, such as water, methanol,ethanol, water/methanol mixtures, or water/ethanol mixtures. Theselection of a suitable solvent is well known and appreciate on the artand depends on the solubility of the bis-alkylhexahydropyrimidinederivative of structure (4) and the polyamine salt of structure (5). Thereaction is carried out at temperatures of from 10° C. to the refluxingtemperature of the solvent. For a bis-alkylhexahydropyrimidinederivatives of structure (4) in which Y is hydrogen it is advantageousto provide for the removal of the formaldehyde which is formed duringthe course of the reaction, such as a sweep of an inert gas over thereaction vessel. A polyamine derivative of structure (5) can be isolatedfrom the reaction zone as the salts thereof by precipitation andfiltration. A compound of structure (5) can be purified as salts thereofby recrystallization.

Compounds of structure (5) can be isolated from their salt by methodswell known in the art. Salts of the compounds of structure (5) can beexchanged as is well known in the art.

The following examples present typical syntheses as described in SchemeA. These examples are understood to be illustrative only and are notintended to limit the scope of the invention in any way. As used in thefollowing examples, the following terms have the meanings indicated: "g"refers to grams, "mmol" refers to millimoles, "mL" refers tomilliliters, "° C." refers to degrees Celsius, "R_(f) " refers toretention factor, "mp" refers to melting point, "dec" refers todecomposition, "M" refers to molar, and "TLC" refers to thin layerchromatography.

EXAMPLE 1

Step a:

1,7-Bis-(hexahydropyrimidin-1-yl)-heptane ##STR8##

Dissolve N,N'-bis-(3-aminopropyl)-1,7-heptanediamine tetrahydrochloridesalt (10.0 g, 25.6 mmol) in an aqueous 1 M sodium hydroxide solution(103 mL, 103 mmol). Cool to 5° C. in an ice-bath. Add an aqueoussolution of formaldehyde (37% by weight, 3.8 mL, 50.8 mmol). Stir in theice-bath for 1 hour and then warm to ambient temperature and stir for 1hour. Extract the aqueous reaction mixture three times withdichloromethane (100 mL). Combine the organic layers and dry over K₂CO₃, filter and evaporate in vacuo to give the title compound as lightyellow solid which can be used without further purification.Chromatograph on silica gel eluting with 3% concentrated aqueous ammoniasolution/methanol to give an analytical sample of the title compound asa white solid: TLC R_(f) =0.46 (silica gel, 5% concentrated aqueousammonia solution/methanol); mp; 52°-53° C. ¹ H NMR (300 MHz, CDCl₃) δ:1.3 (m, 6H), 1.46, (br m, 4H), 1.61 (p, J=5.5 Hz, 4H), 1.7 (br s, 2H),2.21 (dd, J=7.6 Hz J=8.6 Hz, 4H), 2.56 (br t, J=4.8 Hz, 4H), 2.81 (t,J=5.5 Hz, 4H), 3.37 (s, 4H). Elem. Anal. calculated for C₁₅ H₃₂ N₄ : C,67.11; H, 12.02; N, 20.87. Found: C, 66.65; H, 12.85; N, 20.69.

EXAMPLE 2

Step b:

1,7-Bis-(3-acetylhexahydropyrimidin-1-yl)-heptane ##STR9##

Combine 1,7-bis-(hexahydropyrimidinyl-1-yl)-heptane (5.0 g, 18.7 mmol)and triethylamine (7.6 g, 75 mmol) in ethyl acetate (40 mL). Add aceticanhydride (103 mL, 103 mmol) and heat at reflux for 8 hours. Evaporatethe reaction mixture in vacuo to obtain a concentrate. Partition theconcentrate between a 1M aqueous solution of sodium hydroxide (40 mL)and dichloromethane (75 mL). Extract the aqueous layer two times withdichloromethane (75 mL). Combine the organic layers and dry over K₂ CO₃,filter, and evaporate in vacuo to give the title compound as lightorange oil which can be used without further purification. Chromatographon silica gel eluting with 10% methanol/dichloromethane to give ananalytical sample of the title compound as a colorless oil: TLC R_(f)=0.35 (silica gel, 10% methanol/ dichloromethane). ¹ H NMR (300 MHz,CDC1₃) δ: 1.3 (m, 6H), 1.5 (m, 4H), 1.67/1.70 (overlapping, complexpentets, J=5.6/5.6 Hz 4H), 2.09/2.11 (s, 6H), 2.4 (m, 4H), 2.72/2.73 (t,J=6.3/6.3 Hz, 4H), 3.48/3.60 (t, J=5.6/5.6 Hz, 4H), 4.04/4.23 (s, 4H).Elem. Anal. calculated for C₁₉ H₃₆ N₄ 0₂ : C, 64.74; H, 10.29; N, 15.89.Found: C, 63.13; H, 10.59; N, 15.52.

EXAMPLE 3

Step c:

1,7-Bis-(3-ethylhexahydropyrimidin-1-yl)-heptane ##STR10##

Combine lithium aluminum hydride (0.85 g, 22.7 mmol) and anhydroustetrahydrofuran (60 mL). Add to the above suspension a solution of1,7-bis-(3-acetylhexahydropyrimidinyl-1-yl)-heptane (2.0 g, 5.7 mmol)and anhydrous tetrahydrofuran (40 mL). Heat at reflux and stir under aninert atmosphere for 16 hours. Cool to ambient temperature. Carefully,add an saturated aqueous solution of sodium sulfate (5 mL) to quench thereaction. Stir for 16 hours to ensure a complete quench. Filter througha bed of Celite and rinse the filter cake obtained three times withtetrahydrofuran (10 mL). Evaporate the filtrate in vacuo to give aresidue. Dissolve the residue in acetonitrile (50 mL) and concentrate invacuo to give the title compound as an oil which can be used withoutfurther purification. Chromatograph on silica gel eluting with 1/20/80,concentrated aqueous ammonia solution/methanol/dichloromethane to givean analytical sample of the title compound as a colorless oil: TLC R_(f)=0.56 (silica gel, 1/20/80, concentrated aqueous ammoniasolution/methanol/dichloromethane). ¹ H NMR (300 MHz, CDC1₃) δ: 1.07 (t,J=7.2 Hz, 6H), 1.3 (m, 6H), 1.46 (br m, 4H), 1.67 (p, J=5.6 Hz, 4H),2.30 (dd, J=7.6 Hz, J=7.6 Hz, 4H), 2.39 (q, J=7.2 Hz, 4H), 2.40-2.50 (m,8H), 3.08 (br s, 4H). Elem. Anal. calculated for C₁₉ H₄₀ N₄ : C, 70.31;H, 12.42; N, 17.26. Found: C, 69.50; H, 12.75; N, 16.70.

EXAMPLE 4

Step d:

N,N'-Bis- 3-(ethylamino)propyl!-1,7-heptanediamine tetrahydrochloride##STR11##

Combine 1,7-Bis-(3-ethylhexahydropyrimidinyl-1-yl)-heptane (0.50 g, 1.5mmol) and methanol (20 mL). Add aqueous 12 M hydrochloric acid (5 mL).Heat to reflux and provide a sweep of nitrogen above the condenser toremove the formaldehyde that is released in the reaction. Periodicallyreplace the methanol that is lost due to the nitrogen sweep. After 3hours, cool the reaction to ambient temperature and collect the solidprecipitate by filtration. Recrystallize the solid from water (0.8 mL)and 2-propanol (2.9 mL) to give the title compound as a solid; mp: 313°C. (dec); TLC R_(f) =0.39 (silica gel, 40% concentrated aqueous ammoniasolution/methanol). ¹ H NMR (300 MHz, D₂ 0) δ: 1.30 (t, J=7.3 Hz, 6H),1.40 (m, 6H), 1.70 (br p, J=7.3 Hz, 4H), 2.1 (m, 4H), 3.1 (m, 4H), 3.13(q, J=7.3 Hz, 4H), 3.15 (m, 8H). Elem. Anal. calculated for C₁₇ H₄₀ N₄.4HC1: C, 45.74; H, 9.94; N, 12.55; Cl, 31.77. Found: C, 45.49; H, 10.48;N, 12.33, Cl, 31.20.

What is claimed is:
 1. A compound of the formula ##STR12## wherein m is6, 7, 8, or 9,R₁, R₂, R₃, R₄, R₅, and R₆, are each independentlyhydrogen or a C₁ -C₃ alkyl group with the proviso that the total numberof carbon atoms incorporated by all the groups R₁, R₂, R₃, R₄, R₅, or R₆may not exceed 6, Z is hydrogen, methyl, or ethyl, Y is hydrogen, C₁ -C₆alkyl, phenyl, or substituted phenyl.
 2. A compound according to claim 1wherein Y is hydrogen.
 3. A compound according to claim 2 wherein m is7.
 4. A compound according to claim 3 wherein Z is methyl.
 5. A compoundaccording to claim 4 wherein R₁, R₂, R₃, R₄, R₅, and R₆ are hydrogen. 6.A compound of the formula ##STR13## wherein m is 8 or 9,R₁, R₂, R₃, R₄,R₅, and R₆, are each independently hydrogen or a C₁ -C₃ alkyl group withthe proviso that the total number of carbon atoms incorporated by allthe groups R₁, R₂, R₃, R₄, R₅, or R6 may not exceed 6, Z is hydrogen,methyl, or ethyl, Y is hydrogen, C₁ -C₆ alkyl, phenyl, or substitutedphenyl.
 7. A compound according to claim 6 wherein Y is hydrogen.
 8. Acompound according to claim 7 wherein Z is methyl.
 9. A compoundaccording to claim 8 wherein R₁, R₂, R₃, R₄, R₅, and R₆ are hydrogen.